Huth Tobias, Schmidtmayer Johann, Alzheimer Christian, Hansen Ulf-Peter
Department of Physiology, University of Kiel, Olshausenstrasse 40, 24098, Kiel, Germany.
Pflugers Arch. 2008 Oct;457(1):103-19. doi: 10.1007/s00424-008-0500-y. Epub 2008 Apr 19.
Basic principles of the gating mechanisms of neuronal sodium channels, especially the fast inactivation process, were revealed by a quantitative analysis of the effects of the chemically irreversible modifying agent chloramine T. The compound is known to enhance the open probability of sodium channels by interfering with the inactivation process. The key for the deduction of structure-function relationships was obtained from the analysis of single-channel patch-clamp data, especially the finding that chloramine T-induced modification of inactivation occurred in four steps. These steps were termed modes 1-4 (four-mode gating model), and their temporal sequence was always the same. The kinetic analysis of single-channel traces with an improved two-dimensional dwell-time fit revealed the possible mechanism related to each mode. Similarities to the kinetics of the sodium channel mutant F1489Q led to the assignment of modes 1 and 2 to transient defects in the locking of the inactivation particle (hinged lid). In the third mode, the hinged lid was unable to lock permanently. Finally, in mode 4, the apparent single-channel current was reduced, which could be explained by fast gating, presumably related to the selectivity filter.
通过对化学不可逆修饰剂氯胺T作用的定量分析,揭示了神经元钠通道门控机制的基本原理,尤其是快速失活过程。已知该化合物通过干扰失活过程来提高钠通道的开放概率。通过对单通道膜片钳数据的分析,特别是发现氯胺T诱导的失活修饰分四个步骤进行,从而获得了推导结构-功能关系的关键。这些步骤被称为模式1-4(四模式门控模型),其时间顺序总是相同的。用改进的二维驻留时间拟合对单通道记录进行动力学分析,揭示了与每种模式相关的可能机制。与钠通道突变体F1489Q动力学的相似性导致将模式1和2归因于失活颗粒(铰链盖)锁定中的瞬时缺陷。在第三种模式中,铰链盖无法永久锁定。最后,在模式4中,表观单通道电流降低,这可以用快速门控来解释,可能与选择性过滤器有关。